Basic information Uses Safety Supplier Related
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Dansyl chloride

Basic information Uses Safety Supplier Related

Dansyl chloride Basic information

Product Name:
Dansyl chloride
Synonyms:
  • 1-(dimethylamino)-5-naphthalenesulfonylchloride
  • 1-chlorosulfonyl-5-dimethylaminonaphthalene
  • 5-(dimethylamino)-1-naphthalenesulfonylchlorid
  • 5-dimethylaminonaphthyl-5-sulfonylchloride
  • 5-Dimethylamino-1-naphthalenesulphonyl chloride~DNSCl
  • Dansyl chloride 99+ %
  • 5-(N,N-DIMETHYLAMINO)-NAPHTHALENE-1-SULF ONYL CHLORIDE FOR THE FLUORES-CENT-MARK
  • DANSYL CHLORIDE, 98+%
CAS:
605-65-2
MF:
C12H12ClNO2S
MW:
269.75
EINECS:
210-092-6
Product Categories:
  • marker
  • Amines
  • Amino Group Labeling Reagents for Fluorescence HPLC
  • Aromatics
  • Fluorescent Labels & Indicators
  • Sulfur & Selenium Compounds
  • Analytical Chemistry
  • Fluorescence Detection (HPLC Labeling Reagents)
  • HPLC Labeling Reagents
  • Hydroxyl Group Labeling Reagents for Fluorescence HPLC
Mol File:
605-65-2.mol
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Dansyl chloride Chemical Properties

Melting point:
72-74 °C(lit.)
Boiling point:
371.3±22.0 °C(Predicted)
Density 
1.1702 (rough estimate)
refractive index 
1.5630 (estimate)
storage temp. 
2-8°C
solubility 
acetone: 50 mg/mL
form 
powder and chunks
pka
2.38±0.40(Predicted)
color 
yellow to orange
Water Solubility 
Soluble in dimethyl fluoride, acetone, chloroform, pyridine, benzene and dioxane. Insoluble in water.
Sensitive 
Moisture Sensitive
Merck 
14,2814
BRN 
2217205
Stability:
Hygroscopic, Moisture Sensitive
InChIKey
XPDXVDYUQZHFPV-UHFFFAOYSA-N
CAS DataBase Reference
605-65-2(CAS DataBase Reference)
EPA Substance Registry System
1-Naphthalenesulfonyl chloride, 5-(dimethylamino)- (605-65-2)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45-3
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
RTECS 
QK3688000
10-21
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29214980

MSDS

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Dansyl chloride Usage And Synthesis

Uses

Dansyl chloride or 5-Dimethylaminonaphthalene-1-sulfonyl chloride (CAS 605-65-2) is a fluorogenic reagent used for protein, N-terminal amino acid and peptide detection by reverse phase high performance liquid chromatography (HPLC). It is also used to determine the degree of labeling in chymotrypsin and ovalbumin. It acts as a precursor for the synthesis of other derivatives like dansyl amide.
Dansyl chloride is non-fluorescent until it reacts with amines. The resulting Dansyl amides have environmentally sensitive fluorescence quantum yields and emission maxima along with large Stokes shifts. This environment-sensitive fluorescence property has made Dansyl chloride an important tool for biophysical studies.

Chemical Properties

yellow to orange-yellow crystalline powder

Uses

A fluorogenic reagent for N-terminal derivatization of amino acids and peptides and detection by reverse phase HPLC.

Uses

Dansyl chloride is a fluorogenic reagent used for protein, N-terminal amino acid and peptide detection by reverse phase high performance liquid chromatography (HPLC). It is also used to determine the degree of labeling in chymotrypsin and ovalbumin. It acts as a precursor for the synthesis of other derivatives like dansyl amide.

Uses

Reagent for fluorescent labelling of amines, amino acids and proteins.

Uses

In fluorescent labelling, column chromatography, HPLC.

Definition

ChEBI: Dansyl chloride is an aminonaphthalene and a sulfonic acid derivative.

General Description

Dansyl chloride is a fluorogenic reagent which is typically employed for the derivatization of amino acids.

Biochem/physiol Actions

Dansyl chloride is a sulfonyl chloride compound. It is used to end tag amino groups of peptides and proteins. Dansyl chloride is used for derivatization of free amino acids and amines in neural samples and biological fluids. It is used to study fluorescent conjugates of albumin, protein conformational changes studies and active site characterization.

Safety Profile

Poison by intravenous route, When heated to decomposition it emits very toxic fumes of Cland NOx

Dansyl chlorideSupplier

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